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Neuromelanin-targeted 18 F-P3BZA PET/MR imaging of the substantia nigra in rhesus macaques.
Feng, Hongyan; Tu, Ning; Wang, Ke; Ma, Xiaowei; Zhang, Zhentao; Liu, Zhongchun; Cheng, Zhen; Bu, Lihong.
Afiliación
  • Feng H; PET-CT/MRI Center, Renmin Hospital of Wuhan University, 95Zhangzhidong Road, Wuchang District, Wuhan, 430060, Hubei, China.
  • Tu N; PET-CT/MRI Center, Renmin Hospital of Wuhan University, 95Zhangzhidong Road, Wuchang District, Wuhan, 430060, Hubei, China.
  • Wang K; PET-CT/MRI Center, Renmin Hospital of Wuhan University, 95Zhangzhidong Road, Wuchang District, Wuhan, 430060, Hubei, China.
  • Ma X; Department of Nuclear Medicine, Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Zhang Z; Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
  • Liu Z; Department of Psychiatry, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
  • Cheng Z; State Key Laboratory of Drug Research, Molecular Imaging Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China. zcheng@simm.ac.cn.
  • Bu L; PET-CT/MRI Center, Renmin Hospital of Wuhan University, 95Zhangzhidong Road, Wuchang District, Wuhan, 430060, Hubei, China. bulihongs@126.com.
EJNMMI Res ; 14(1): 79, 2024 Sep 03.
Article en En | MEDLINE | ID: mdl-39225971
ABSTRACT

BACKGROUND:

Neuromelanin is mostly located in dopaminergic neurons in the substantia nigra (SN) pars compacta, and can be detected by magnetic resonance imaging (MRI). It is a promising imaging-base biomarker for neurological diseases. We previously developed a melanin-specific probe N-(2-(diethylamino)-ethyl)-18F-5-fluoropicolinamide (18F-P3BZA), which was initially developed for the imaging of melanoma. 18F-P3BZA exhibited high levels of binding to the melanin in vitro and in vivo with high retention and favorable pharmacokinetics. In this study we further investigated whether 18F-P3BZA could be used to quantitatively detect neuromelanin in the SN in healthy rhesus macaques.

RESULTS:

18F-P3BZA exhibited desired hydrophobicity with estimated log Know 5.08 and log D7.4 1.68. 18F-P3BZA readily crossed the blood-brain barrier with brain transport coefficients (Kin) of 40 ± 8 µL g-1s-1. 18F-P3BZA accumulated specifically in neuromelanotic PC12 cells, melanin-rich melanoma cells, and melanoma xenografts. Binding of 18F-P3BZA to B16F10 cells was much higher than to SKOV3 cells at 60 min (6.17 ± 0.53%IA and 0.24 ± 0.05%IA, respectively). In the biodistribution study, 18F-P3BZA had higher accumulation in B16F10 tumors (6.31 ± 0.99%IA/g) than in SKOV3 tumors (0.25 ± 0.09%IA/g). Meanwhile, 18F-P3BZA uptake in B16F10 tumors could be blocked by excess cold 19F-P3BZA (0.81 ± 0.02%IA/g, 88% inhibition, p < 0.05). PET/MRI 18F-P3BZA provided clear visualization of neuromelanin-rich SN at 30-60 min after injection in healthy macaques. The SN to cerebella ratios were 2.7 and 2.4 times higher at 30 and 60 min after injection. In in vitro autoradiography studies 18F-P3BZA exhibited high levels of binding to the SN, and almost no binding to surrounding midbrain tissues.

CONCLUSION:

18F-P3BZA PET/MRI clearly images neuromelanin in the SN, and may assist in the early diagnosis of neurological diseases associated with abnormal neuromelanin expression.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: EJNMMI Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: EJNMMI Res Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania